NP-MRD: Showing NP-Card for Talaroenamine E (NP0014745)

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Record Information

Version

2.0

Created at

2021-01-05 23:49:57 UTC

Updated at

2021-07-15 17:18:06 UTC

NP-MRD ID

NP0014745

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Talaroenamine E

Provided By

NPAtlas

Description

Talaroenamine E belongs to the class of organic compounds known as methoxyphenols. Methoxyphenols are compounds containing a methoxy group attached to the benzene ring of a phenol moiety. Talaroenamine E is found in Talaromyces stipitatus and Talaromyces stipitatus ATCC 10500. Based on a literature review very few articles have been published on Talaroenamine E.

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306242120063D          

 39 40  0  0  0  0            999 V2000
   -4.3848    2.6417    1.0874 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0962    2.1968    0.6540 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9970    0.9142    0.1334 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0656    0.0515    0.0121 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9066   -1.2300   -0.5202 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0164   -2.0538   -0.6180 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6793   -1.6730   -0.9405 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5978   -0.8113   -0.8223 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7723    0.4524   -0.2938 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5497    1.3072   -0.2067 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6153    0.7309   -0.6665 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5885    0.0532   -0.3111 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6141   -0.2869   -1.3454 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2864   -0.1849   -2.5462 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9633   -0.7265   -0.9579 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8982    0.4669   -0.7523 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4605   -1.5616   -1.9535 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9095   -1.4997    0.3128 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7449   -2.4274    0.4652 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9230   -1.1766    1.3201 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8439   -0.4477    1.0045 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9129   -0.1840    2.1115 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1194    2.6103    0.2714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7262    1.9135    1.8673 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2581    3.6356    1.5215 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0414    0.3703    0.3333 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6200   -2.0819   -1.4352 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5254   -2.6573   -1.3558 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6310   -1.1592   -1.1530 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7886    2.2583   -0.7867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4757    1.6234    0.8536 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7105    0.2139   -0.0541 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3411    0.7466   -1.7307 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2916    1.3208   -0.3777 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0296   -1.3085   -2.8008 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0867   -1.5404    2.3249 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1722   -0.8397    3.0016 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9694    0.8412    2.5247 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1100   -0.4983    1.8289 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  6  0  0  0
 15 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
  9  3  1  0  0  0  0
 21 12  1  0  0  0  0
  1 23  1  0  0  0  0
  1 24  1  0  0  0  0
  1 25  1  0  0  0  0
  4 26  1  0  0  0  0
  6 27  1  0  0  0  0
  7 28  1  0  0  0  0
  8 29  1  0  0  0  0
 10 30  1  0  0  0  0
 10 31  1  0  0  0  0
 16 32  1  0  0  0  0
 16 33  1  0  0  0  0
 16 34  1  0  0  0  0
 17 35  1  0  0  0  0
 20 36  1  0  0  0  0
 22 37  1  0  0  0  0
 22 38  1  0  0  0  0
 22 39  1  0  0  0  0
M  END

     RDKit          3D

 39 40  0  0  0  0  0  0  0  0999 V2000
   -4.3848    2.6417    1.0874 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0962    2.1968    0.6540 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9970    0.9142    0.1334 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0656    0.0515    0.0121 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9066   -1.2300   -0.5202 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0164   -2.0538   -0.6180 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6793   -1.6730   -0.9405 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5978   -0.8113   -0.8223 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7723    0.4524   -0.2938 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5497    1.3072   -0.2067 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6153    0.7309   -0.6665 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5885    0.0532   -0.3111 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6141   -0.2869   -1.3454 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2864   -0.1849   -2.5462 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9633   -0.7265   -0.9579 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8982    0.4669   -0.7523 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4605   -1.5616   -1.9535 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9095   -1.4997    0.3128 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7449   -2.4274    0.4652 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9230   -1.1766    1.3201 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8439   -0.4477    1.0045 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9129   -0.1840    2.1115 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1194    2.6103    0.2714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7262    1.9135    1.8673 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2581    3.6356    1.5215 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0414    0.3703    0.3333 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6200   -2.0819   -1.4352 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5254   -2.6573   -1.3558 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6310   -1.1592   -1.1530 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7886    2.2583   -0.7867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4757    1.6234    0.8536 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7105    0.2139   -0.0541 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3411    0.7466   -1.7307 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2916    1.3208   -0.3777 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0296   -1.3085   -2.8008 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0867   -1.5404    2.3249 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1722   -0.8397    3.0016 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9694    0.8412    2.5247 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1100   -0.4983    1.8289 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  5  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 13 15  1  0
 15 16  1  0
 15 17  1  6
 15 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  2  0
 21 22  1  0
  9  3  1  0
 21 12  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  4 26  1  0
  6 27  1  0
  7 28  1  0
  8 29  1  0
 10 30  1  0
 10 31  1  0
 16 32  1  0
 16 33  1  0
 16 34  1  0
 17 35  1  0
 20 36  1  0
 22 37  1  0
 22 38  1  0
 22 39  1  0
M  END


  Mrv1652306242120063D          

 39 40  0  0  0  0            999 V2000
   -4.3848    2.6417    1.0874 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0962    2.1968    0.6540 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9970    0.9142    0.1334 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0656    0.0515    0.0121 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9066   -1.2300   -0.5202 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0164   -2.0538   -0.6180 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6793   -1.6730   -0.9405 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5978   -0.8113   -0.8223 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7723    0.4524   -0.2938 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5497    1.3072   -0.2067 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.6153    0.7309   -0.6665 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5885    0.0532   -0.3111 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6141   -0.2869   -1.3454 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2864   -0.1849   -2.5462 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9633   -0.7265   -0.9579 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8982    0.4669   -0.7523 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4605   -1.5616   -1.9535 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9095   -1.4997    0.3128 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7449   -2.4274    0.4652 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9230   -1.1766    1.3201 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8439   -0.4477    1.0045 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9129   -0.1840    2.1115 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1194    2.6103    0.2714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7262    1.9135    1.8673 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2581    3.6356    1.5215 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0414    0.3703    0.3333 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6200   -2.0819   -1.4352 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5254   -2.6573   -1.3558 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6310   -1.1592   -1.1530 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7886    2.2583   -0.7867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4757    1.6234    0.8536 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7105    0.2139   -0.0541 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3411    0.7466   -1.7307 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2916    1.3208   -0.3777 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0296   -1.3085   -2.8008 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0867   -1.5404    2.3249 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1722   -0.8397    3.0016 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9694    0.8412    2.5247 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1100   -0.4983    1.8289 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  6  0  0  0
 15 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
  9  3  1  0  0  0  0
 21 12  1  0  0  0  0
  1 23  1  0  0  0  0
  1 24  1  0  0  0  0
  1 25  1  0  0  0  0
  4 26  1  0  0  0  0
  6 27  1  0  0  0  0
  7 28  1  0  0  0  0
  8 29  1  0  0  0  0
 10 30  1  0  0  0  0
 10 31  1  0  0  0  0
 16 32  1  0  0  0  0
 16 33  1  0  0  0  0
 16 34  1  0  0  0  0
 17 35  1  0  0  0  0
 20 36  1  0  0  0  0
 22 37  1  0  0  0  0
 22 38  1  0  0  0  0
 22 39  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0014745

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C([H])C([H])=C(C(OC([H])([H])[H])=C1[H])C([H])([H])\N=C1\C(=O)[C@](O[H])(C(=O)C([H])=C1C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C16H17NO5/c1-9-6-13(19)16(2,21)15(20)14(9)17-8-10-4-5-11(18)7-12(10)22-3/h4-7,18,21H,8H2,1-3H3/b17-14+/t16-/m1/s1

> <INCHI_KEY>
IATGCYDWADNGPJ-MRXNPFEDSA-N

> <FORMULA>
C16H17NO5

> <MOLECULAR_WEIGHT>
303.314

> <EXACT_MASS>
303.110672651

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
31.104112466990422

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R,6E)-2-hydroxy-6-{[(4-hydroxy-2-methoxyphenyl)methyl]imino}-2,5-dimethylcyclohex-4-ene-1,3-dione

> <ALOGPS_LOGP>
1.89

> <JCHEM_LOGP>
2.635862565666667

> <ALOGPS_LOGS>
-3.22

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.465505523211505

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.432986780297716

> <JCHEM_PKA_STRONGEST_BASIC>
1.9320625738010961

> <JCHEM_POLAR_SURFACE_AREA>
96.19

> <JCHEM_REFRACTIVITY>
81.17469999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.83e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R,6E)-2-hydroxy-6-{[(4-hydroxy-2-methoxyphenyl)methyl]imino}-2,5-dimethylcyclohex-4-ene-1,3-dione

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 39 40  0  0  0  0  0  0  0  0999 V2000
   -4.3848    2.6417    1.0874 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0962    2.1968    0.6540 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9970    0.9142    0.1334 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0656    0.0515    0.0121 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9066   -1.2300   -0.5202 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0164   -2.0538   -0.6180 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6793   -1.6730   -0.9405 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5978   -0.8113   -0.8223 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7723    0.4524   -0.2938 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5497    1.3072   -0.2067 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6153    0.7309   -0.6665 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5885    0.0532   -0.3111 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6141   -0.2869   -1.3454 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2864   -0.1849   -2.5462 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9633   -0.7265   -0.9579 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8982    0.4669   -0.7523 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4605   -1.5616   -1.9535 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9095   -1.4997    0.3128 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7449   -2.4274    0.4652 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9230   -1.1766    1.3201 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8439   -0.4477    1.0045 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9129   -0.1840    2.1115 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1194    2.6103    0.2714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7262    1.9135    1.8673 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2581    3.6356    1.5215 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0414    0.3703    0.3333 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6200   -2.0819   -1.4352 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5254   -2.6573   -1.3558 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6310   -1.1592   -1.1530 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7886    2.2583   -0.7867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4757    1.6234    0.8536 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7105    0.2139   -0.0541 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3411    0.7466   -1.7307 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2916    1.3208   -0.3777 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0296   -1.3085   -2.8008 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0867   -1.5404    2.3249 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1722   -0.8397    3.0016 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9694    0.8412    2.5247 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1100   -0.4983    1.8289 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  5  7  2  0
  7  8  1  0
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  9 10  1  0
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 22 38  1  0
 22 39  1  0
M  END

HEADER    PROTEIN                                 24-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-JUN-21         0                                  
HETATM    1  C   UNK     0      -4.385   2.642   1.087  0.00  0.00           C+0
HETATM    2  O   UNK     0      -3.096   2.197   0.654  0.00  0.00           O+0
HETATM    3  C   UNK     0      -2.997   0.914   0.133  0.00  0.00           C+0
HETATM    4  C   UNK     0      -4.066   0.052   0.012  0.00  0.00           C+0
HETATM    5  C   UNK     0      -3.907  -1.230  -0.520  0.00  0.00           C+0
HETATM    6  O   UNK     0      -5.016  -2.054  -0.618  0.00  0.00           O+0
HETATM    7  C   UNK     0      -2.679  -1.673  -0.941  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.598  -0.811  -0.822  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.772   0.452  -0.294  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.550   1.307  -0.207  0.00  0.00           C+0
HETATM   11  N   UNK     0       0.615   0.731  -0.667  0.00  0.00           N+0
HETATM   12  C   UNK     0       1.589   0.053  -0.311  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.614  -0.287  -1.345  0.00  0.00           C+0
HETATM   14  O   UNK     0       2.286  -0.185  -2.546  0.00  0.00           O+0
HETATM   15  C   UNK     0       3.963  -0.727  -0.958  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.898   0.467  -0.752  0.00  0.00           C+0
HETATM   17  O   UNK     0       4.460  -1.562  -1.954  0.00  0.00           O+0
HETATM   18  C   UNK     0       3.910  -1.500   0.313  0.00  0.00           C+0
HETATM   19  O   UNK     0       4.745  -2.427   0.465  0.00  0.00           O+0
HETATM   20  C   UNK     0       2.923  -1.177   1.320  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.844  -0.448   1.004  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.913  -0.184   2.111  0.00  0.00           C+0
HETATM   23  H   UNK     0      -5.119   2.610   0.271  0.00  0.00           H+0
HETATM   24  H   UNK     0      -4.726   1.914   1.867  0.00  0.00           H+0
HETATM   25  H   UNK     0      -4.258   3.636   1.522  0.00  0.00           H+0
HETATM   26  H   UNK     0      -5.041   0.370   0.333  0.00  0.00           H+0
HETATM   27  H   UNK     0      -5.620  -2.082  -1.435  0.00  0.00           H+0
HETATM   28  H   UNK     0      -2.525  -2.657  -1.356  0.00  0.00           H+0
HETATM   29  H   UNK     0      -0.631  -1.159  -1.153  0.00  0.00           H+0
HETATM   30  H   UNK     0      -0.789   2.258  -0.787  0.00  0.00           H+0
HETATM   31  H   UNK     0      -0.476   1.623   0.854  0.00  0.00           H+0
HETATM   32  H   UNK     0       5.710   0.214  -0.054  0.00  0.00           H+0
HETATM   33  H   UNK     0       5.341   0.747  -1.731  0.00  0.00           H+0
HETATM   34  H   UNK     0       4.292   1.321  -0.378  0.00  0.00           H+0
HETATM   35  H   UNK     0       4.030  -1.309  -2.801  0.00  0.00           H+0
HETATM   36  H   UNK     0       3.087  -1.540   2.325  0.00  0.00           H+0
HETATM   37  H   UNK     0       1.172  -0.840   3.002  0.00  0.00           H+0
HETATM   38  H   UNK     0       0.969   0.841   2.525  0.00  0.00           H+0
HETATM   39  H   UNK     0      -0.110  -0.498   1.829  0.00  0.00           H+0
CONECT    1    2   23   24   25                                             
CONECT    2    1    3                                                       
CONECT    3    2    4    9                                                  
CONECT    4    3    5   26                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5   27                                                       
CONECT    7    5    8   28                                                  
CONECT    8    7    9   29                                                  
CONECT    9    8   10    3                                                  
CONECT   10    9   11   30   31                                             
CONECT   11   10   12                                                       
CONECT   12   11   13   21                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   17   18                                             
CONECT   16   15   32   33   34                                             
CONECT   17   15   35                                                       
CONECT   18   15   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   36                                                  
CONECT   21   20   22   12                                                  
CONECT   22   21   37   38   39                                             
CONECT   23    1                                                            
CONECT   24    1                                                            
CONECT   25    1                                                            
CONECT   26    4                                                            
CONECT   27    6                                                            
CONECT   28    7                                                            
CONECT   29    8                                                            
CONECT   30   10                                                            
CONECT   31   10                                                            
CONECT   32   16                                                            
CONECT   33   16                                                            
CONECT   34   16                                                            
CONECT   35   17                                                            
CONECT   36   20                                                            
CONECT   37   22                                                            
CONECT   38   22                                                            
CONECT   39   22                                                            
MASTER        0    0    0    0    0    0    0    0   39    0   80    0
END

RDKit          3D

39 40  0  0  0  0  0  0  0  0999 V2000
   -4.3848    2.6417    1.0874 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0962    2.1968    0.6540 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9970    0.9142    0.1334 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0656    0.0515    0.0121 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9066   -1.2300   -0.5202 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0164   -2.0538   -0.6180 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6793   -1.6730   -0.9405 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5978   -0.8113   -0.8223 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7723    0.4524   -0.2938 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5497    1.3072   -0.2067 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6153    0.7309   -0.6665 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5885    0.0532   -0.3111 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6141   -0.2869   -1.3454 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2864   -0.1849   -2.5462 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9633   -0.7265   -0.9579 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8982    0.4669   -0.7523 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4605   -1.5616   -1.9535 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9095   -1.4997    0.3128 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7449   -2.4274    0.4652 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9230   -1.1766    1.3201 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8439   -0.4477    1.0045 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9129   -0.1840    2.1115 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1194    2.6103    0.2714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7262    1.9135    1.8673 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2581    3.6356    1.5215 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0414    0.3703    0.3333 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6200   -2.0819   -1.4352 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5254   -2.6573   -1.3558 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6310   -1.1592   -1.1530 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7886    2.2583   -0.7867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4757    1.6234    0.8536 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7105    0.2139   -0.0541 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3411    0.7466   -1.7307 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2916    1.3208   -0.3777 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0296   -1.3085   -2.8008 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0867   -1.5404    2.3249 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1722   -0.8397    3.0016 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9694    0.8412    2.5247 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1100   -0.4983    1.8289 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  5  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
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 15 17  1  6
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  9  3  1  0
 21 12  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  4 26  1  0
  6 27  1  0
  7 28  1  0
  8 29  1  0
 10 30  1  0
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 16 32  1  0
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 17 35  1  0
 20 36  1  0
 22 37  1  0
 22 38  1  0
 22 39  1  0
M  END

View in JSmol View NMR Assignments

Synonyms

Not Available

Chemical Formula

C₁₆H₁₇NO₅

Average Mass

303.3140 Da

Monoisotopic Mass

303.11067 Da

IUPAC Name

(2R,6E)-2-hydroxy-6-{[(4-hydroxy-2-methoxyphenyl)methyl]imino}-2,5-dimethylcyclohex-4-ene-1,3-dione

Traditional Name

(2R,6E)-2-hydroxy-6-{[(4-hydroxy-2-methoxyphenyl)methyl]imino}-2,5-dimethylcyclohex-4-ene-1,3-dione

CAS Registry Number

Not Available

SMILES

COC1=C(CN=C2C(C)=CC(=O)[C@@](C)(O)C2=O)C=CC(O)=C1

InChI Identifier

InChI=1S/C16H17NO5/c1-9-6-13(19)16(2,21)15(20)14(9)17-8-10-4-5-11(18)7-12(10)22-3/h4-7,18,21H,8H2,1-3H3/t16-/m1/s1

InChI Key

IATGCYDWADNGPJ-MRXNPFEDSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Talaromyces stipitatus	LOTUS Database	35616633
Talaromyces stipitatus ATCC 10500	NPAtlas	26386982

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as methoxyphenols. Methoxyphenols are compounds containing a methoxy group attached to the benzene ring of a phenol moiety.

Kingdom

Super Class

Class

Sub Class

Direct Parent

Alternative Parents

Substituents

Methoxyphenol
Phenoxy compound
Methoxybenzene
Quinone
Phenol ether
M-benzoquinone
Anisole
1-hydroxy-2-unsubstituted benzenoid
Cyclohexenone
Alkyl aryl ether
Monocyclic benzene moiety
Acyloin
Tertiary alcohol
Secondary ketimine
Azomethine
Cyclic ketone
Ketone
Ketimine
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Ether
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Imine
Carbonyl group
Alcohol
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	1.89	ALOGPS
logP	2.64	ChemAxon
logS	-3.2	ALOGPS
pKa (Strongest Acidic)	9.43	ChemAxon
pKa (Strongest Basic)	1.93	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	96.19 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	81.17 m³·mol⁻¹	ChemAxon
Polarizability	31.1 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

NPAtlas ID

NPA006311

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

78442007

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

139584870

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Talaroenamine E (NP0014745)

MOL for NP0014745 (Talaroenamine E)

3D MOL for NP0014745 (Talaroenamine E)

3D SDF for NP0014745 (Talaroenamine E)

3D-SDF for NP0014745 (Talaroenamine E)

PDB for NP0014745 (Talaroenamine E)

3D PDB for NP0014745 (Talaroenamine E)

SMILES for NP0014745 (Talaroenamine E)

INCHI for NP0014745 (Talaroenamine E)

Structure for NP0014745 (Talaroenamine E)

3D Structure for NP0014745 (Talaroenamine E)